A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539466



Internal ID20912761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:48225826..48227367hg38UCSC Ensembl
chr1:48691498..48693039hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg381542
hg191542
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251169
Samples
Known GenesSLC5A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539466
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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